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3328-70-9

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3328-70-9 Usage

General Description

4-Hydroxyisophthalaldehyde (4-HIPA) is a chemical compound that belongs to the class of aldehydes and contains a hydroxyl group at the 4 position of the aromatic ring. It is commonly used as a starting material in the synthesis of various pharmaceuticals, agrochemicals, and organic compounds due to its versatile reactivity. 4-HIPA is also a key building block in the production of complex organic molecules and is valued for its ability to undergo various chemical reactions, such as condensation, oxidation, and reduction, to yield a wide range of functionalized derivatives. Its unique structure and reactivity make it a valuable intermediate in the chemical industry for the preparation of diverse organic compounds. Additionally, 4-HIPA has potential applications in the development of new materials and in catalysis due to its unique chemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 3328-70-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,2 and 8 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3328-70:
(6*3)+(5*3)+(4*2)+(3*8)+(2*7)+(1*0)=79
79 % 10 = 9
So 3328-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H6O3/c9-4-6-1-2-8(11)7(3-6)5-10/h1-5,11H

3328-70-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxybenzene-1,3-dicarbaldehyde

1.2 Other means of identification

Product number -
Other names 3-formyl-4-hydroxybenzaldehyde

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3328-70-9 SDS

3328-70-9Relevant articles and documents

A nitroreductase and glutathione responsive nanoplatform for integration of gene delivery and near-infrared fluorescence imaging

Barz, Matthias,Bi, Qunjie,Chen, Xiaobing,Hu, Ao,Jin, Rongrong,Ke, Bowen,Liang, Hong,Nie, Yu,Song, Xu

, p. 6949 - 6952 (2020)

A novel platform rationally integrating indocyanine green analogues and an arginine-rich dendritic peptide with both nitroreductase (NTR) and glutathione (GSH) reduction responsive linkers was developed. This multifunctional platform can enable selective

Fluorescent probe for fluorine ion detection, application of fluorescent probe and method for detecting fluorine ions in to-be-detected sample

-

Paragraph 0047; 0051; 0056-0057, (2021/08/06)

The invention belongs to the technical field of analytical chemistry, and particularly relates to a fluorescent probe for fluorine ion detection, application of the fluorescent probe and a method for detecting fluorine ions in a to-be-detected sample. The invention provides a compound as shown in a formula I, or an optical isomer or salt thereof, and provides application of the compound as a fluorine ion detection fluorescent probe. According to the method for detecting the fluorine ions in the to-be-detected sample, the compound, or the optical isomer or the salt of the compound is used as a fluorine ion detection fluorescent probe for detection. The fluorescent probe has the advantages of good water solubility, high selectivity, high response speed, low detection limit, good stability, wide applicable pH range and good application prospect.

Synthesis, characterization, and UV–visible study of some new photochromic formyl-containing 1′,3′,3′-trimethylspiro[chromene-2,2′-indoline] derivatives

Sepehr, Zeinalabedin,Nasr-Isfahani, Hossein,Mahdavian, Ali Reza,Amin, Amir Hossein

, p. 3061 - 3067 (2021/05/27)

The spiropyran derivatives can exist in two forms, the closed-ring spiropyran form and the open-ring merocyanine (MC) form. The SP form could be converted into the MC form upon UV irradiation. In this work, some 1′,3′,3′-trimethylspiro[chromene-2,2′-indoline] derivatives containing the nitro and formyl groups are synthesized via the reaction of 1,3,3-trimethyl-2-methylene-5-nitroindoline with the corresponding salicylaldehyde derivatives. These compounds have different photochromic behaviors. The synthesized photochromic molecules are characterized by the FT-IR, 1H-NMR, and 13C-NMR spectroscopic techniques. In order to investigate the photochromic properties of these compounds, the UV–visible spectroscopic analyses of their methanolic solutions before and after exposure to a UV lamp (in the spectral range of 360–400?nm) are studied. Graphic abstract: [Figure not available: see fulltext.].

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